Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population
Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., Csurhes, Peter, Pender, Michael P., & Griffiths, Lyn R. (2004) Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population. Journal of the Neurological Sciences, 218(1-2), pp. 25-28.
Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases (NOS) are a family of enzymes that control the production of nitric oxide. It is possible that neuronal NOS could be involved in MS pathophysiology and hence the nNOS gene is a potential candidate for involvement in disease susceptibility. The aim of this study was to determine whether allelic variation at the nNOS gene locus is associated with MS in an Australian cohort. DNA samples obtained from a Caucasian Australian population affected with MS and an unaffected control population, matched for gender, age and ethnicity, were genotyped for a microsatellite polymorphism in the promoter region of the nNOS gene. Allele frequencies were compared using chi-squared based statistical analyses with significance tested by Monte Carlo simulation. Allelic analysis of MS cases and controls produced a chi-squared value of 5.63 with simulated P = 0.96 (OR(max) = 1.41, 95% CI: 0.926-2.15). Similarly, a Mann-Whitney U analysis gave a non-significant P-value of 0.377 for allele distribution. No differences in allele frequencies were observed for gender or clinical course subtype (P > 0.05). Statistical analysis indicated that there is no association of this nNOS variant and MS and hence the gene does not appear to play a genetically significant role in disease susceptibility.
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|Item Type:||Journal Article|
|Divisions:||Current > Institutes > Institute of Health and Biomedical Innovation|
|Copyright Owner:||Copyright 2004 Elsevier BV|
|Deposited On:||20 Sep 2013 04:56|
|Last Modified:||02 Jul 2014 23:04|
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